A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5774238



Internal ID9459993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99723812..99724314hg38UCSC Ensembl
chr15:100264017..100264519hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670359
Supporting Variants
SamplesNA18910
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5774238
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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